ClinVar Miner

List of variants in gene MFSD6L reported as uncertain significance for not specified

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_152599.4(MFSD6L):c.769G>C (p.Glu257Gln) rs372929205 0.00038
NM_152599.4(MFSD6L):c.1642G>C (p.Glu548Gln) rs144825375 0.00027
NM_152599.4(MFSD6L):c.988G>A (p.Val330Ile) rs374041366 0.00027
NM_152599.4(MFSD6L):c.1540G>A (p.Val514Met) rs143689038 0.00019
NM_152599.4(MFSD6L):c.64G>A (p.Val22Met) rs200206293 0.00016
NM_152599.4(MFSD6L):c.1345T>C (p.Ser449Pro) rs369773529 0.00013
NM_152599.4(MFSD6L):c.1723T>G (p.Trp575Gly) rs540324838 0.00013
NM_152599.4(MFSD6L):c.413C>G (p.Ser138Cys) rs750932704 0.00010
NM_152599.4(MFSD6L):c.895G>A (p.Val299Met) rs201466404 0.00010
NM_152599.4(MFSD6L):c.967C>G (p.His323Asp) rs367887663 0.00009
NM_152599.4(MFSD6L):c.1621A>G (p.Ile541Val) rs766992966 0.00008
NM_152599.4(MFSD6L):c.368G>C (p.Gly123Ala) rs368610174 0.00008
NM_152599.4(MFSD6L):c.77G>A (p.Arg26Gln) rs149429543 0.00007
NM_152599.4(MFSD6L):c.268G>A (p.Ala90Thr) rs775689714 0.00006
NM_152599.4(MFSD6L):c.1249C>T (p.Leu417Phe) rs201568333 0.00005
NM_152599.4(MFSD6L):c.1321C>T (p.Leu441Phe) rs373817865 0.00005
NM_152599.4(MFSD6L):c.497G>A (p.Arg166His) rs377452108 0.00005
NM_152599.4(MFSD6L):c.983C>T (p.Ser328Leu) rs200102201 0.00004
NM_152599.4(MFSD6L):c.1505G>C (p.Ser502Thr) rs140422131 0.00003
NM_152599.4(MFSD6L):c.154A>G (p.Met52Val) rs139030153 0.00003
NM_152599.4(MFSD6L):c.293C>G (p.Pro98Arg) rs976542781 0.00003
NM_152599.4(MFSD6L):c.934T>C (p.Phe312Leu) rs772912507 0.00003
NM_152599.4(MFSD6L):c.244G>T (p.Gly82Cys) rs372028955 0.00002
NM_152599.4(MFSD6L):c.1103T>A (p.Leu368His) rs370096466 0.00001
NM_152599.4(MFSD6L):c.1535G>C (p.Gly512Ala) rs1325567200 0.00001
NM_152599.4(MFSD6L):c.1658A>G (p.Tyr553Cys) rs1448807946 0.00001
NM_152599.4(MFSD6L):c.259T>G (p.Ser87Ala) rs1156830491 0.00001
NM_152599.4(MFSD6L):c.545C>T (p.Thr182Ile) rs1327689059 0.00001
NM_152599.4(MFSD6L):c.917T>C (p.Val306Ala) rs1222443922 0.00001
NM_152599.4(MFSD6L):c.985G>A (p.Val329Met) rs776916906 0.00001
NM_152599.4(MFSD6L):c.100C>A (p.Leu34Met)
NM_152599.4(MFSD6L):c.1235T>G (p.Leu412Arg)
NM_152599.4(MFSD6L):c.1317C>G (p.Ser439Arg)
NM_152599.4(MFSD6L):c.1339T>C (p.Tyr447His)
NM_152599.4(MFSD6L):c.1343A>C (p.Tyr448Ser) rs1038384884
NM_152599.4(MFSD6L):c.1502G>T (p.Gly501Val) rs192487452
NM_152599.4(MFSD6L):c.1548G>A (p.Met516Ile) rs2544807631
NM_152599.4(MFSD6L):c.1550G>A (p.Arg517His)
NM_152599.4(MFSD6L):c.1586T>C (p.Val529Ala) rs2087008469
NM_152599.4(MFSD6L):c.160A>C (p.Thr54Pro) rs2544809087
NM_152599.4(MFSD6L):c.1669C>G (p.Leu557Val)
NM_152599.4(MFSD6L):c.197G>A (p.Cys66Tyr)
NM_152599.4(MFSD6L):c.203T>G (p.Phe68Cys)
NM_152599.4(MFSD6L):c.370G>A (p.Val124Ile)
NM_152599.4(MFSD6L):c.425C>T (p.Ala142Val)
NM_152599.4(MFSD6L):c.466C>T (p.Pro156Ser)
NM_152599.4(MFSD6L):c.505C>T (p.His169Tyr)
NM_152599.4(MFSD6L):c.586G>T (p.Asp196Tyr) rs2544808559
NM_152599.4(MFSD6L):c.644G>T (p.Gly215Val) rs749727387
NM_152599.4(MFSD6L):c.653G>A (p.Gly218Glu)
NM_152599.4(MFSD6L):c.686A>G (p.Lys229Arg)
NM_152599.4(MFSD6L):c.71G>A (p.Gly24Glu) rs754890444
NM_152599.4(MFSD6L):c.727C>T (p.Arg243Trp)
NM_152599.4(MFSD6L):c.768G>T (p.Trp256Cys)
NM_152599.4(MFSD6L):c.790G>A (p.Glu264Lys)
NM_152599.4(MFSD6L):c.856A>C (p.Ser286Arg) rs1354948323
NM_152599.4(MFSD6L):c.941T>A (p.Met314Lys)
NM_152599.4(MFSD6L):c.95C>G (p.Pro32Arg)
NM_152599.4(MFSD6L):c.982T>A (p.Ser328Thr) rs2544808194

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